Label: INTOMEDI FIRST AMPOULE EGF- adenosine liquid

  • NDC Code(s): 82879-0003-1, 82879-0003-2
  • Packager: Janytree Inc.
  • Category: HUMAN OTC DRUG LABEL

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Drug Label Information

Updated July 12, 2022

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  • INACTIVE INGREDIENTS

    Water, Ethyl Ascorbyl Ether, Dipropylene Glycol, Glycerin, 1,2-Hexanediol, Lactobacillus/Hydrolyzed
    Pea Seed Extract Ferment Filtrate(Bio-Peptone®), Butylene Glycol, Dimethyl Sulfone, Centella Asiatica
    Extract, Panthenol, Pentylene Glycol, Mentha Piperita (Peppermint) Extract, Hydrolyzed Collagen, Sodium
    Hyaluronate, Allantoin, Polygonum Cuspidatum Root Extract, Scutellaria Baicalensis Root
    Extract, Camellia Sinensis Leaf Extract, Glycyrrhiza Glabra (Licorice) Root Extract, Sodium Hyaluronate
    Crosspolymer, Chamomilla Recutita (Matricaria) Flower Extract, Rosmarinus Officinalis (Rosemary) Leaf
    Extract, Acetyl Hexapeptide-8(AHP-8), Copper Tripeptide-1(CTP-1), sh-Oligopeptide-1(EGF:1ppm)

  • ACTIVE INGREDIENTS

    adenosine

  • PURPOSE

    An intensive skin energy ampoule for a younger, healthier-looking skin
    Formulated with different growth factors and our patented Bio-Peptone®

  • WARNINGS

    For external use only When using this product
    ■ If following abnormal symptoms occurs after using the product, stop using the product and consult with a skin specialist. Symptoms : Red specks, swelling, itching
    ■ Do not use on the skin parts affected by wound, eczema, or dermatitis.
    Keep out of reach of children.
    ■ If swallowed, get a medical help or contact a person in control center immediately.
    ■ Avoid contact with eyes.

  • KEEP OUT OF REACH OF CHILDREN

    KEEP OUT OF REACH OF CHILDREN

    If swallowed, get a medical help or contact a person in control center immediately.

  • INDICATIONS & USAGE

    apply a proper amount to the skin, and massage gently until fully absorbed

  • DOSAGE & ADMINISTRATION

    for external use only

  • PRINCIPAL DISPLAY PANEL

    label

  • INGREDIENTS AND APPEARANCE
    INTOMEDI FIRST AMPOULE EGF 
    adenosine liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:82879-0003
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ADENOSINE (UNII: K72T3FS567) (ADENOSINE - UNII:K72T3FS567) ADENOSINE0.04 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:82879-0003-25 in 1 PACKAGE07/13/2022
    1NDC:82879-0003-15 mL in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other07/13/2022
    Labeler - Janytree Inc. (688403840)
    Registrant - Janytree Inc. (688403840)
    Establishment
    NameAddressID/FEIBusiness Operations
    Janytree Inc.688403840manufacture(82879-0003)
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